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Kcnt1tm1.2Clin
Targeted Allele Detail
Summary
Symbol: Kcnt1tm1.2Clin
Name: potassium channel, subfamily T, member 1; targeted mutation 1.2, Christopher J Lingle
MGI ID: MGI:5908121
Gene: Kcnt1  Location: Chr2:25753807-25808285 bp, + strand  Genetic Position: Chr2, 18.27 cM
Alliance: Kcnt1tm1.2Clin page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:228059
Parent Cell Line:  Not Specified (ES Cell)
Strain of Origin:  C57BL/6 x 129X1/SvJ
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsA targeting vector was designed to insert a loxP site upstream of exon 11 and a second loxP site, followed by an FRT-flanked neomycin resistance (neo) cassette which includes a third loxP site, downstream of exon 11. Recombinase-mediated recombination removed the FRT-flanked neo cassette and exon 11. (J:228059)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Kcnt1 Mutation:  67 strains or lines available
References
Original:  J:228059 Martinez-Espinosa PL, et al., Knockout of Slo2.2 enhances itch, abolishes KNa current, and increases action potential firing frequency in DRG neurons. Elife. 2015;4:e10013
All:  3 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory